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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 8411-8418 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 66 (1995), S. 4649-4654 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: An UV multipass optical absorption method to increase the sensitivity for radical species detection has been developed for high temperature chemical kinetics experiments in a shock tube. The specific illustration is for OH radicals in the reflected shock wave regime. With a resonance lamp source, 12 optical passes were found to give a sufficient signal-to-noise ratio for a large range of [OH]. Two different calibration procedures using the reaction systems H2/O2 and C2H5I/NO2 were used, and a curve of growth was determined. The measured absorbance (ABS), was found to be dependent on both temperature and [OH]. The results can be expressed in a modified Beer's law form as,(ABS)=9.49×10−12T−0.5281[OH]0.8736.Using this curve of growth, the absorbance data from the above kinetics experiments were converted to concentration profiles. These were fully modeled with previously established mechanisms, giving excellent fits. The multipass method is compared to earlier systems that used both resonance lamp and laser absorption sources, and the increase in sensitivity is found to be substantial due primarily to the increased path length. This increased sensitivity inhibits the effects of any possible secondary chemistry thereby allowing chemically isolated experiments on OH + molecules to be performed at high temperatures. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0301-0104
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Optics Communications 61 (1987), S. 257-260 
    ISSN: 0030-4018
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0649
    Keywords: 34.00 ; 36.00 ; 82.40
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The Vibrational Predissociation (VP) lifetimes and dissociation channels are reported for the van der Waals complexes p-DiFluoroBenzene-Ar (pDFB-Ar), pDFB-N2 and p-FluoroToluene-Ar (pFT-Ar). The dissociation occurs on theS 1 potential energy surface after excitation of an S1 ring breathing level with εvib ≈ 800 cm−1. Trends are observed in the lifetimes and dissociation channels as the experiments move among the complexes. The VP characteristics of pFT-Ar are most distinctive. As opposed to all other aromatic complexes, pFT-Ar has little VP channel selectivity. These complexes are members of a set chosen to explore the VP vibrational dynamics by systematic changes of complex level structure. The change from pDFB-Ar to pDFB-N2 introduces nearly free internal rotation in the complex partner and an additional van der Waals mode. pFT-Ar introduces a nearly free internal rotation attached directly to the ring. We discuss how these changes may be related to the observed VP dynamics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 29 (1997), S. 535-543 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The recently developed I-atom atomic resonance absorption spectrometric(ARAS) technique has been used to study the thermal decomposition kinetics of CH3I over the temperature range, 1052-1820 K. Measured rate constants for CH3I(+Kr)→CH3+I(+Kr) between 1052 and 1616 K are best expressed by k(±36%)=4.36×10-9 exp(-19858 K/T) cm3 molecule-1 s-1. Two unimolecular theoretical approaches were used to rationalize the data. The more extensive method, RRKM analysis, indicates that the dissociation rates are effectively second-order, i.e., the magnitude is 61-82% of the low-pressure-limit rate constants over 1052-1616 K and 102-828 torr. With the known E0=ΔH00=55.5 kcal mole -1, the optimized RRKM fit to the ARAS data requires (ΔE)down=590 cm-1. © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 535-543, 1997.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 30 (1998), S. 859-867 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Br-atom atomic resonance absorption spectrometry (ARAS) has been developed and applied to measure thermal decomposition rate constants for CF3Br (+ Kr)→CF3+Br (+ Kr) over the temperature range, 1222-1624 K. The Br-atom curve-of-growth (145〈λ〈163 nm) was determined using this reaction. For [Br]≤1×1012 molecules cm-3, absorbance, (ABS)=1.410×10-13 [Br], yielding σ=1.419×10-14 cm2. The curve-of-growth was then used to convert (ABS) to Br-atom profiles which were then analyzed to give measured rate constants. These can be expressed in second-order by k1=8.147×10-9 exp(-24488 K/T) cm3 molecule-1 s-1 (±33%, 1222≤T≤1624 K). A unimolecular theoretical approach was used to rationalize the data. Theory indicates that the dissociation rates are closer to second- than to first-order, i.e., the magnitudes are 30-53% of the low-pressure-limit rate constants over 1222-1624 K and 123-757 torr. With the known, E0=ΔH00=70.1 kcal mole-1, the optimized theoretical fit to the ARAS data requires 〈ΔE〉down=550 cm-1. These conclusions are consistent with recently published data and theory from Kiefer and Sathyanarayana. © 1998 John Wiley & Sons, Inc. Int J Chem Kinet 30: 859-867, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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