RELATIVE RATE CONSTANTS FOR REACTION OF OH RADICAL WITH SULFURIC ACID FORMIC ACID AND CEROUS ION

1956 ◽  
Vol 78 (8) ◽  
pp. 1768-1769 ◽  
Author(s):  
Thomas J. Sworski
Keyword(s):  
Sulfuric Acid ◽  
Formic Acid ◽  
Rate Constants ◽  
Relative Rate ◽  
Oh Radical ◽  
Relative Rate Constants

Specific Rate Constants of Hydroxyl Radical and Hydrated Electron Reactions Determined by the RCL Method

1976 ◽  
Vol 31 (11) ◽  
pp. 1501-1510 ◽  
Author(s):  
W. A. Prütz ◽  
S. Vogel
Keyword(s):  
Rate Constants ◽  
Relative Rate ◽  
Published Data ◽  
Oh Radicals ◽  
Specific Rate ◽  
Oh Radical ◽  
X Irradiation ◽  
Relative Rate Constants ◽  
Pseudo Halides ◽  
Common Application

Relative rate constants of OH radical and eaq- reactions have been determined by comparing, under steady x-irradiation, the effect of various solutes upon the radiationinduced chemiluminescence (RCL) of aqueous dye (DH) solutions, [DH + ·OH] + eaq- → DH* + OH-. The results abundantly confirm other published data. RCL changes upon addition of phosphates indicate prototropic reactions with the oxidized dye, D·+ H2PO4- ⇌ DH·+ + HPO42-, promoting or inhibiting the formation of semioxidized dye (DH·+) as the most efficient RCL precursor. The RCL enhancement commonly observed upon addition of halides and pseudo halides is discussed at some length on the base of previous and present results in order to focus attention to the possible correlation between such RCL enhancement and the effect of halogen-sensitization in radiobiology. RCL results suggest that the halide transients formed from OH radicals, X- + ·OH → X· + OH-, are very powerful oxidizing agents reacting with aromatics by electron-abstraction rather than by addition or H-abstraction. The common application of I- and SCN- as competitors for the estimation of OH radical reactivities is being commented in the context

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.

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.

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.

Sign in / Sign up

Export Citation Format

Share Document