Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Chemistry  (3)
Material
Years
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 111-122 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate of CH4 disappearance in a shock-heated CH4:D2:Ar = 9.70:9.86:80.44 mixture was monitored by coincidence absorption of the 2948 cm-1 He-Ne laser line over the shockfront temperature range of 1900-2300K. Comparison with CH4 pyrolysis results by means of computer simulations suggested that atom and free radical chains are responsible for the homogeneous D/H exchange reaction on CH4.Additional simulations for the experimental conditions of previous single-pulse shock tube experiments led to the recognition of a high sensitivity of the exchange rate to trace amounts of hydrocarbon impurity and to the dissociation rate of CH4.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 23-44 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The decomposition of C2H6 in Ar was studied by laser-absorption and laser-schlieren measurements of the reaction rate behind incident shock waves with 1300 〈 T 〈 2500°K and 1.1 〈 ρ 〈 4.4 × 10-6 mol/cm3. The experimental profiles were parameterized by suitable measures of reaction progress. Computer simulations using a 14-reaction mechanism were used to compare assumptions about rate constant expressions with the experimental parameters and to investigate the sensitivity of computed parameters to these assumptions. A rate constant expression k(cm3/mol·sec) = 2 × 10111 T-25.26 exp(-80 320/T) was found for the primary dissociation step C2H6 + M = CH3 + CH3 + M under the conditions studied; no difference in rate was discernable between M = Ar and M = C2H6. Rate constant expressions found to be suitable for the remaining reactions of the mechanism, to some of which the computed parameters were sensitive, were in accord with previous proposals. Our results and results from earlier investigations of the primary decomposition reaction, in both forward and reverse directions, were extrapolated, using RRK methods, to obtain low-pressure limiting rate constants and found to be concordant.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 503-517 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The recombination of carbon monoxide and oxygen atoms was studied in reflected shock waves in H2:O2:CO:Ar = 0.1:1:24:75 with 1300 〈 T5 2200 K and 2 〈 P5 〈 4 atm. Reaction progress was monitored by observations of the carbon monoxide flame spectrum near 435 nm and carbon dioxide thermal emission near 4.2 μm. Data analysis was accomplished with the aid of computer modeling using a 27-reaction mechanism. Computer modeling experiments also showed that these measurements were sensitive primarily to the rate of the reaction CO + O + M = CO2 + M and only slightly sensitive to the rates of other reactions. The best fit to the data was achieved with a rate constant for this reaction of 7.7 × 10-35 exp[19 kJ/RT] cm6 s for the temperature range of these experiments. Correlation of this result and previous data covering the temperature range 250 〈 T 〈 11,000 K confirms that this recombination reaction is governed by a nonadiabatic curve crossing with an activation barrier of about 20 kJ and subsequent deactivation of a singlet CO2 molecule.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...