Bibliothek

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
Filter
  • Chemistry  (9)
Materialart
Erscheinungszeitraum
Schlagwörter
  • 1
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 19 (1987), S. 457-486 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A chemical kinetic reaction mechanism has been developed which describes the oxidation of propanal within the temperature range 400-700 K. This mechanism has been tested against data obtained by four experimental groups over a wide range of initial conditions. The induction period and the absolute rate of propanal consumption are predicted to within a factor of 2 for initial densities of oxygen and propanal ranging over factors of 400. The existence and location of the negative temperature coefficient in the consumption of propanal are also simulated properly. The yields of all major and most minor products are predicted to within a factor of 2 for the wide variety of initial conditions tested. Sensitivity analyses were carried out at 553 and 713 K to identify the reactions primarily responsible for controlling the rate of propanal consumption and the distribution of products.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 24 (1992), S. 179-189 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The pressure dependence of reaction (1), Cl + C2H2 + M → C2H2Cl + M, has been measured by a relative rate technique using the pressure independent abstraction reaction (2), Cl + C2H6 → C2H5 + HCl, as the reference. Values of k1/k2 were measured at pressures between 25 and 1300 torr at four temperatures ranging from 252 to 370 K, using air, N2, or SF6 diluent gases. Low pressure measurements (10-50 torr) were performed at 230 K. Assuming a temperature-independent center broadening factor of 0.6 in the Troe formalism and using the established value of k2, these data can be used to determine the temperature dependent high and low pressure limiting rate constants over the range of conditions studied in air for reaction (1): k∞(1) = 2.13 × 10-10 (T/300)-1.045 cm3/molecule-s; and k0(1) = 5.4 × 10-30 (T/300)-2.09 cm6/molecule2-s. Use of these expressions yields rate constants with an estimated 20% accuracy including uncertainty in the reference reaction. The data indicate that the rate constant for a typical stratospheric condition at 30 km altitude is approximately 50% of that previously estimated.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 29 (1997), S. 43-55 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Absolute (flash photolysis) and relative (FTIR-smog chamber and GC) rate techniques were used to study the gas-phase reactions of Cl atoms with C2H6 (k1), C3H8 (k3), and n-C4H10 (k2). At 297 ± 1 K the results from the two relative rate techniques can be combined to give k2/k1 = (3.76 ± 0.20) and k3/k1 = (2.42 ± 0.10). Experiments performed at 298-540 K give k2/k1 = (2.0 ± 0.1)exp((183 ± 20)/T). At 296 K the reaction of Cl atoms with C3H8 produces yields of 43 ± 3% 1-propyl and 57 ± 3% 2-propyl radicals, while the reaction of Cl atoms with n-C4H10 produces 29 ± 2% 1-butyl and 71 ± 2% 2-butyl radicals. At 298 K and 10-700 torr of N2 diluent, 1- and 2-butyl radicals were found to react with Cl2 with rate coefficients which are 3.1 ± 0.2 and 2.8 ± 0.1 times greater than the corresponding reactions with O2. A flash-photolysis technique was used to measure k1 = (5.75 ± 0.45) × 10-11 and k2 = (2.15 ± 0.15) × 10-10 cm3 molecule-1 s-1 at 298 K, giving a rate coefficient ratio k2/k1 = 3.74 ± 0.40, in excellent agreement with the relative rate studies. The present results are used to put other, relative rate measurements of the reactions of chlorine atoms with alkanes on an absolute basis. It is found that the rate of hydrogen abstraction from a methyl group is not influenced by neighboring groups. The results are used to refine empirical approaches to predicting the reactivity of Cl atoms towards hydrocarbons. Finally, relative rate methods were used to measure rate coefficients at 298 K for the reaction of Cl atoms with 1- and 2-chloropropane and 1- and 2-chlorobutane of (4.8 ± 0.3) × 10-11, (2.0 ± 0.1) × 10-10, (1.1 ± 0.2) &times 10-10, and (7.0 ± 0.8) × 10-11 cm3 molecule-1 s-1, respectively. © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 43-55, 1997.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 997-1012 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The oxidation of propionaldehyde has been investigated in a 1-L Pyrex reactor at total pressures of 50-120 torr and temperatures 553-713 K. Detection of reactants and products was principally by molecular beam mass spectrometry, although certain species could only be measured by gas-chromatographic analysis. At 553 K the yield of water was ∼83% of the propionaldehyde consumed, leading to the conclusion that OH is the principal chain carrier near the beginning of the negative temperature coefficient region. Many oxygenated organics (CH2O, CH3CHO, C2H5OH, C2H5O2H, CH3O2H) and C2H4 are formed during the oxidation process. These oxidation products are consistent with the important role of O2 addition to C2H5 radicals at 553 K followed by subsequent reactions of the C2H5O2 radical. As the temperature is increased, the product concentrations smoothly change to a much simpler distribution in which C2H4, H2O2, and CO are the dominant products.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 5
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 21 (1989), S. 1113-1122 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Using Fourier transform infrared spectroscopy, the ethene yield from the reaction of C2H5 radicals with O2 has been determined to be 1.50 ± 0.09%, 0.85 ± 0.11%, and 〈0.1% at total pressures of 25, 50, and 700 torr, respectively. Additionally, the rate constant of the reaction of C2H5 radicals with molecular chlorine was measured relative to that with molecular oxygen. A ratio k6/k7 = 1.99 ± 0.14 was measured at 700 torr total pressure which, together with the literature value of k7 = 4.4 × 10-12 cm3 molecule-1s-1, yields k6 = (8.8 ± 0.6) × 10-12 cm3 molecule-1s-1. Quoted errors represent 2σ. These results are discussed with respect to previous kinetic and mechanistic studies of C2H5 radicals.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 27 (1995), S. 205-218 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The kinetics of the gas-phase reaction of Cl atoms with CF3I have been studied relative to the reaction of Cl atoms with CH4 over the temperature range 271-363 K. Using k(Cl + CH4) = 9.6 × 10-12 exp(-2680/RT) cm3 molecule-1 s-1, we derive k(Cl + CF3I) = 6.25 × 10-11 exp(-2970/RT) in which Ea has units of cal mol-1. CF3 radicals are produced from the reaction of Cl with CF3I in a yield which was indistinguishable from 100%. Other relative rate constant ratios measured at 296 K during these experiments were k(Cl + C2F5I)/k(Cl + CF3I) = 11.0 ± 0.6 and k(Cl + C2F5I)/k(Cl + C2H5Cl) = 0.49 ± 0.02. The reaction of CF3 radicals with Cl2 was studied relative to that with O2 at pressures from 4 to 700 torr of N2 diluent. By using the published absolute rate constants for k(CF3 + O2) at 1-10 torr to calibrate the pressure dependence of these relative rate constants, values of the low- and high-pressure limiting rate constants have been determined at 296 K using a Troe expression: k0(CF3 + O2) = (4.8 ± 1.2) × 10-29 cm6 molecule-2 s-1; k∞(CF3 + O2) = (3.95 ± 0.25) × 10-12 cm3 molecule-1 s-1; Fc = 0.46. The value of the rate constant k(CF3 + Cl2) was determined to be (3.5 ± 0.4) × 10-14 cm3 molecule-1 s-1 at 296 K. The reaction of Cl atoms with CF3I is a convenient way to prepare CF3 radicals for laboratory study. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 25 (1993), S. 667-680 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Relative rate experiments using UV photolysis of F2 or Cl2 have been used to determine rate constant ratios for several hydrofluorocarbon (HFC) reactions with Cl or F atoms and for HFC alkyl radicals with molecular halogens. For mixtures with F2 present, dark reactions are, also, observed which are attributed to thermal dissociation of the F2 to form F atoms. At 296 K, the rate of reaction (1a) [CF2HCH3 + F → CF2CH3 + HF] relative to (1b) [CF2HCH3 + F → CF2HCH2 + HF] is k1a/k1b = 0.73 (±0.13) and is independent of T (= 262-348 K). At 296 K, the ratio of reaction (2a) [CF2HCH2F + F → products] to that of (k1a + k1b) is (k1a + k1b)/k2a = 2.7 (±0.4), and for reaction (2b) [CF3CH3 + F → products] (k1a + k1b)/k2b = 22 ± 12. The temperature dependence (263-365 K) of the rate constant of reaction (3) [CF3CFH2 + Cl → products] relative to reaction (4) [CF3CFClH + Cl → products] is k3/k4(±10%) = 1.55 exp(-300 K/T). For the alkyl radicals formed from HFC 152a (CF2HCH2 and CF2CH3) and from HFC 134a (CF3CFH), rate constants for the reactions with F2 and Cl2 were measured relative to their reactions with O2. The rate constant of reaction (5cl) [CF2CH3 + Cl2 → CF2ClCH3 + Cl] relative to (5o) [CF2CH3 + O2 → CF2(O2)CH3] is k5cl/k5o(±15%) = 0.3 exp(200 K/T). For reaction (5f) [CF2CH3 + F2 → CF3CH3 + F], k5f/k5o(±35%) = 0.23. The ratio for reaction (6f) [CF2HCH2 + F2 → CF2HCH2F + F] relative to (6o) [CF2HCH2 + O2 → CF2HCH2O2] is k6f/k6o(±40%) = 1.23 exp(-730 K/T). The rate constant ratio for reaction (8cl) [CF3CFH + Cl2 → CF3CFClH + Cl] relative to reaction (8o) [CF3CFH + O2 → CF3CFHO2] is k8cl/k8o(±18%) = 0.16 exp(-940 K/T). For reaction (8f) [CF3CFH + F2 → CF3CF2H + F], k8f/k8o(±35%) = 0.6 exp(-860 K/T). © 1993 John Wiley & Sons, Inc.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 28 (1996), S. 627-635 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The kinetics and mechanism of the gas-phase reaction of Cl atoms with CH2CO have been studied with a FTIR spectrometer/smog chamber apparatus. Using relative rate methods the rate of reaction of Cl atoms with ketene was found to be independent of total pressure over the range 1-700 torr of air diluent with a rate constant of (2.7 ± 0.5) × 10-10 cm3 molecule-1 s-1 at 295 K. The reaction proceeds via an addition mechanism to give a chloroacetyl radical (CH2ClCO) which has a high degree of internal excitation and undergoes rapid unimolecular decomposition to give a CH2Cl radical and CO. Chloroacetyl radicals were also produced by the reaction of Cl atoms with CH2ClCHO; no decomposition was observed in this case. The rates of addition reactions are usually pressure dependent with the rate increasing with pressure reflecting increased collisional stabilization of the adduct. The absence of such behavior in the reaction of Cl atoms with CH2CO combined with the fact that the reaction rate is close to the gas kinetic limit is attributed to preferential decomposition of excited CH2ClCO radicals to CH2Cl radicals and CO as products as opposed to decomposition to reform the reactants. As part of this work ab initio quantum mechanical calculations (MP2/6-31G(d,p)) were used to derive ΔfH298(CH2ClCO) = -(5.4 ± 4.0) kcal mol-1. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 9
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 18 (1986), S. 655-688 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Acetaldehyde oxidation has been studied in experiments at temperatures of 553 and 713 K carried out in a low pressure, static reactor and in numerical modeling calculations using a detailed chemical kinetic reaction mechanism. The results of the experimental study were used to construct and validate the reaction mechanism, which was then used to examine acetaldehydeoxidation in the negative temperature coefficient regime between 550 and 900 K. This mechanism was also tested against independent measurements of acetaldehyde oxidation carried out by Baldwin, Matchan, and Walker. The overall rate of reaction and the properties of the negative temperature coefficient regime were found to be sensitive to the competition between radical decomposition reactions and the addition of molecular oxygen to acetyl and methyl radicals, including particularly \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CH}_{\rm 3} + {\rm O}_2 + {\rm M = CH}_{\rm 3} {\rm O}_{\rm 2} + {\rm M} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CH}_{\rm 3} {\rm CO} + {\rm M = CH}_{\rm 3} {\rm + CO} + {\rm M} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CH}_{\rm 3} {\rm CO} + {\rm O}_{\rm 2} {\rm = CH}_{\rm 3} {\rm CO}_{\rm 3} $$\end{document} During these experiments, an upper limit to the rate of decomposition ofCH3O2H was measured at 553 K. Implications of the results for future kinetic modeling of engine knock are discussed.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...