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Vibrational excitation in atmospheri...
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Reynard, Linda Michelle.
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Vibrational excitation in atmospheric chemistry: Production of hydroxyl in the mesosphere and overtone-driven photochemistry of trifluoroacetic acid.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Vibrational excitation in atmospheric chemistry: Production of hydroxyl in the mesosphere and overtone-driven photochemistry of trifluoroacetic acid./
Author:
Reynard, Linda Michelle.
Description:
95 p.
Notes:
Source: Masters Abstracts International, Volume: 41-03, page: 0791.
Contained By:
Masters Abstracts International41-03.
Subject:
Chemistry, Physical. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=MQ73854
ISBN:
061273854X
Vibrational excitation in atmospheric chemistry: Production of hydroxyl in the mesosphere and overtone-driven photochemistry of trifluoroacetic acid.
Reynard, Linda Michelle.
Vibrational excitation in atmospheric chemistry: Production of hydroxyl in the mesosphere and overtone-driven photochemistry of trifluoroacetic acid.
- 95 p.
Source: Masters Abstracts International, Volume: 41-03, page: 0791.
Thesis (M.Sc.)--University of Toronto (Canada), 2002.
The role of vibrations in the atmosphere has been explored in two cases.
ISBN: 061273854XSubjects--Topical Terms:
560527
Chemistry, Physical.
Vibrational excitation in atmospheric chemistry: Production of hydroxyl in the mesosphere and overtone-driven photochemistry of trifluoroacetic acid.
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Reynard, Linda Michelle.
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Vibrational excitation in atmospheric chemistry: Production of hydroxyl in the mesosphere and overtone-driven photochemistry of trifluoroacetic acid.
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95 p.
500
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Source: Masters Abstracts International, Volume: 41-03, page: 0791.
500
$a
Adviser: D. J. Donaldson.
502
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Thesis (M.Sc.)--University of Toronto (Canada), 2002.
520
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The role of vibrations in the atmosphere has been explored in two cases.
520
$a
A new mechanism for OH production in the mesosphere is assessed. Vibrationally excited H<sub>2</sub>, formed by the collisional energy transfer from <math> <f> <rm>O<inf>2</inf><fen lp="par"><g>S</g><sup>+</sup><inf><mit> g</mit></inf><sup loc="pre">1</sup><rp post="par"></fen></rm> </f> </math>, reacts with O(<super>3</super>P) to yield OH. This contributes 16% to the total OH production at 100 km altitude.
520
$a
Overtone-induced chemistry of trifluoroacetic acid is considered. The elimination of HF is the lowest energy dissociation pathway [50.3 kcal mol<super> −1</super> (MP2/6-311G(2d,p))]. The second fragment forms a stable fluorinated epoxide, CF<sub>2</sub>CO<sub>2</sub>. The absorption cross sections of the <italic> v</italic><sub>OH</sub> = 3, 4, 5 overtones are (2.70 ± 0.09) × 10<super>−20</super>, (1.68 ± 0.19) × 10<super>−21 </super>, and ∼1.5 × 10<super>−22</super> cm<super>2</super> molec<super>−1</super> cm<super>−1</super>, respectively. Excitation to the <italic>v</italic><sub>OH</sub> = 5 or 6 leads to dissociation; the rate constants are 3.7 × 10<super>−9</super> and 2.5 × 10<super> −10</super> s<super>−1</super>, respectively. The overtone-driven photodissociation is more important than the ultraviolet photodissociation in the troposphere, but is insignificant in comparison to wet deposition and reaction with OH.
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School code: 0779.
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Chemistry, Physical.
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University of Toronto (Canada).
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Masters Abstracts International
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41-03.
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Donaldson, D. J.,
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http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=MQ73854
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