Relative rate constants for removal of vibrationally excited OH(X2?i)v=9 by some small molecules at room temperature

1983 ◽  
Vol 15 (2) ◽  
pp. 151-165 ◽  
Author(s):  
B. J. Finlayson-pitts ◽  
D. W. Toohey ◽  
M. J. Ezell
Keyword(s):  
Small Molecules ◽  
Rate Constants ◽  
Room Temperature ◽  
Relative Rate ◽  
Vibrationally Excited ◽  
Relative Rate Constants

REACTION OF OXYGEN ATOMS WITH BUTADIENE

1960 ◽  
Vol 38 (11) ◽  
pp. 2187-2195 ◽  
Author(s):  
R. J. Cvetanović ◽  
L. C. Doyle
Keyword(s):  
Pressure Dependence ◽  
Rate Constants ◽  
Room Temperature ◽  
Relative Rate ◽  
Excess Energy ◽  
General Mechanism ◽  
Arrhenius Parameters ◽  
Heats Of Reaction ◽  
Relative Rate Constants ◽  
Oxygen Atoms

Reaction of oxygen atoms with 1,3-butadiene has been investigated at room temperature. It is found that it conforms to the general mechanism established previously for the analogous reactions of monoolefins. Only 1,2-addition occurs, and the addition products, butadiene monoxide and 3-butenal, possess excess energy when formed as a result of high heats of reaction. The pressure dependence of the formation of the addition products yields the values of the "lifetimes" of the initially produced "hot" molecules. The relative rate constants have been determined at 25 and 127 °C and from these the relative values of the Arrhenius parameters have been calculated.

Vibrational energy distribution in HF formed by elimination from activated CH3CF3 and CH2CF2

1970 ◽  
Vol 48 (18) ◽  
pp. 2919-2930 ◽  
Author(s):  
P. N. Clough ◽  
J. C. Polanyi ◽  
R. T. Taguchi
Keyword(s):  
Rate Constants ◽  
Vibrational Energy ◽  
Flow System ◽  
Relative Rate ◽  
Elimination Reaction ◽  
Vibrationally Excited ◽  
Vibrational Levels ◽  
Relative Rate Constants ◽  
Fast Flow ◽  
Vibrational Energy Distribution

The combination–elimination reaction CH3 + CF3 → CH3CF3† → CH2CF2 + HF has been studied in a fast-flow system. Infrared chemiluminescence arising from the HF product has been observed from vibrational levels v = 1–4, and relative rate constants, k(v), have been obtained for HF formation in these levels. A study has also been made of the reaction CH2CF2 + Hg*(63P1) → CHCF + HF + Hg(61S0), which has been found to produce vibrationally-excited HF. Relative rate constants k(v) for vibrational levels v = 1–4 have been obtained. It appears that channelling of the potential energy into HF vibration, in the course of the elimination step, is more efficient in the first than in the second of these reactions. In the second reaction HF is eliminated with considerable rotational excitation.

The relative rate constants of oxygen, O(3P), atoms with different gaseous unsaturated compounds at room temperature

1986 ◽  
Vol 64 (9) ◽  
pp. 1925-1929 ◽  
Author(s):  
H. Deslauriers ◽  
G. J. Collin
Keyword(s):  
Double Bond ◽  
Rate Constants ◽  
Room Temperature ◽  
Relative Rate ◽  
Unsaturated Hydrocarbon ◽  
Ionization Potentials ◽  
Total Rate ◽  
Simple Method ◽  
Unsaturated Compounds ◽  
Relative Rate Constants

A simple method is proposed in order to measure the relative rate constants of the interactions between oxygen O(3P) atoms and unsaturated hydrocarbon. A 147 nm photolysis of air is used to produce the O(3P) atoms. In the presence of 1,2-butadiene, these oxygen atoms have a very clean reaction that gives rise to propylene formation. By including a suitable additive, and by looking at the formation of propene versus the [additive]/[1,2-butadiene] ratio, the absolute values of the various O(3P) + unsaturated hydrocarbon interactions can be evaluated. These rate constants increase with the number of substituents attached to the double bond. Moreover, a correlation between the total rate constants and ionization potentials is also observed.

Kinetics of the successive chlorination of 1,2-dichloroethane in the liquid phase

1969 ◽  
Vol 22 (6) ◽  
pp. 1177 ◽  
Author(s):  
DS Caines ◽  
RB Paton ◽  
DA Williams ◽  
PR Wilkinson
Keyword(s):  
Liquid Phase ◽  
Rate Constants ◽  
Relative Rate ◽  
Stirred Tank ◽  
Continuous Stirred Tank Reactor ◽  
Alternative Pathways ◽  
Tank Reactor ◽  
Relative Rate Constants ◽  
Continuous Stirred Tank ◽  
Kinetics Of

Liquid 1,2-dichloroethane has been chlorinated by dissolved chlorine to a succession of chloroethanes up to the ultimate hexachloroethane. The results of both batch and continuous stirred tank reactor systems have been analysed by computer techniques to give a set of relative rate constants from which one can predict the product composition for a given chlorine uptake, the aim in this work being to optimize the production of tetrachloroethanes. An unusual feature of the kinetics is that 1,1,1,2- and 1,1,2,2-tetrachloroethanes provide alternative pathways between 1,1,2-trichloroethane and pentachloroethane.

RECOMBINATION OF OPPOSITELY CHARGED AQUEOUS CLUSTER IONS USING ELECTROSTATICALLY MERGED ION BEAMS

1996 ◽  
Vol 03 (01) ◽  
pp. 655-660 ◽  
Author(s):  
B. PLASTRIDGE ◽  
K.A. COWEN ◽  
D.A. WOOD ◽  
M.H. COHEN ◽  
J.V. COE
Keyword(s):  
Rate Constants ◽  
Cluster Size ◽  
Collision Energy ◽  
Relative Rate ◽  
Center Of Mass ◽  
Cluster Ions ◽  
Charged Cluster ◽  
Relative Rate Constants ◽  
Oppositely Charged ◽  
Electrostatic Quadrupole

A new method for studying cluster-cluster interactions is introduced which involves merging mass-selected beams of oppositely charged cluster ions with an electrostatic quadrupole deflector. Recombination is monitored by measuring the rate of fast neutral production. Relative rate constants have been measured for the reaction of H 3O+( H 2 O )n+ OH −( H 2 O )m as a function of cluster size (m=n=0–3), which display a pronounced enhancement with clustering. Relative rate constants have also been measured as a function of center-of-mass collision energy for a heavily clustered reaction (n=3, m=3) and a lightly clustered reaction (n=1, m=0) revealing that clustering produces a dramatic change in the reaction mechanism.

Untersuchung konkurrierender Reaktionen in strömenden Kohlenwasserstoff-Gemischen / Investigation of Competing Reactions in Flowing Mixtures of Hydrocarbons

1974 ◽  
Vol 29 (4) ◽  
pp. 642-649 ◽  
Author(s):  
R. Laupert ◽  
G. von Bünau
Keyword(s):  
Rate Constants ◽  
Atomic Hydrogen ◽  
Relative Rate ◽  
Experimental Conditions ◽  
Kinetic Evaluation ◽  
Alkyl Radicals ◽  
Relative Rate Constants ◽  
Flow Apparatus ◽  
Competing Reactions

The reactions of atomic hydrogen with propene, butene-2, and trimethylethylene, and with mixtures of these olefins with ethylene have been studied using flow apparatus. It was found that under the experimental conditions intermediate alkyl radicals reacted practically only with atomic hydrogen. This made possible a kinetic evaluation of the results yielding numerical values of several relative rate constants of competing intermediate reactions.

Hydrogen Isotope Exchange in 2-Butanone. Further Measurements and Some Comments

1972 ◽  
Vol 50 (19) ◽  
pp. 3239-3241 ◽  
Author(s):  
R. A. Cox ◽  
J. W. Thorpe ◽  
J. Warkentin
Keyword(s):  
Acetic Acid ◽  
Temperature Dependence ◽  
Rate Constants ◽  
Hydrogen Isotope ◽  
Isotope Exchange ◽  
Relative Rate ◽  
Aqueous Media ◽  
Acetate Buffer ◽  
Isokinetic Temperature ◽  
Relative Rate Constants

The ratio of rate constants for exchange at the methylene and methyl positions of butanone, [Formula: see text], is shown to be near 1.69 in 1:1 acetic acid–acetate buffer; nearly twice the value (0.86) for deuterioxide catalysis at 54.8°. Methods of obtaining rate constants for acetate catalysis from composite rates (acetate and deuterioxide), or from rates in buffered media, are shown to be adequate for estimating rate ratios.Detailed temperature dependence of the relative rate constants for either system is not yet available but the effects are known to be small. For butanone enolizations the isokinetic temperature is in the neighborhood of 35°, when reaction is catalyzed by deuterioxide in aqueous media.

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