Relative rate constants for reactions of hydroxyl radicals from the reaction of Fe(II) or Ti(III) with H2O2

1969 ◽  
Vol 47 (20) ◽  
pp. 3737-3744 ◽  
Author(s):  
W. A. Armstrong

In an attempt to clarify the reactions of ferrous sulfate and titanous sulfate with hydrogen peroxide, a novel method has been developed to determine the relative rate constants for reactions of the oxidizing species generated in these systems. These species react with hydrogen peroxide to give perhydroxyl radicals which combine with titanium(IV) ions to form the relatively stable TiOO•3+ radical. This radical gives a strong electron spin resonance signal and the competition between hydrogen peroxide and a scavenger for the oxidizing species can be followed by measuring the amplitude of this signal in the presence of various concentrations of scavenger. The relative rate constants calculated in this way for both the Fe(II)–H2O2 and Ti(III)–H2O2 systems at pH 1.0 agree with those reported for the reactions of hydroxyl radicals in γ-irradiated thymine solutions. This supports the view that hydroxyl radicals are formed in these cases.Under conditions of acidity favoring the hydrolysis of Fe(II) to FeOH+ ions, hydroxyl radical scavengers do not compete with hydrogen peroxide for the precursors of the TiOO•3+ radical. It is suggested that the FeOH+ ions react with hydrogen peroxide to give a different oxidizing species, possibly the ferryl ion.Scavengers investigated were thymine, methanol, ethanol, formic acid, acetic acid, chloride ion, and several amino acids.

2006 ◽  
Vol 40 (14) ◽  
pp. 4460-4466 ◽  
Author(s):  
Hilla Shemer ◽  
Charles M. Sharpless ◽  
Michael S. Elovitz ◽  
Karl G. Linden

1969 ◽  
Vol 22 (6) ◽  
pp. 1177 ◽  
Author(s):  
DS Caines ◽  
RB Paton ◽  
DA Williams ◽  
PR Wilkinson

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.


1996 ◽  
Vol 03 (01) ◽  
pp. 655-660 ◽  
Author(s):  
B. PLASTRIDGE ◽  
K.A. COWEN ◽  
D.A. WOOD ◽  
M.H. COHEN ◽  
J.V. COE

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.


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