Radiation Chemistry Studies with Cyclotron Beams of Variable Energy: Yields in Aerated Ferrous Sulfate Solution1

1957 ◽  
Vol 79 (7) ◽  
pp. 1565-1572 ◽  
Author(s):  
Robert H. Schuler ◽  
Augustine O. Allen
Keyword(s):  
Ferrous Sulfate ◽  
Radiation Chemistry ◽  
Variable Energy

Radiation Chemistry of the Ferrous Sulfate-Benzoic Acid-Xylenol Orange System

1978 ◽  
Vol 75 (2) ◽  
pp. 269 ◽  
Author(s):  
B. L. Gupta ◽  
R. M. Bhat ◽  
K. R. Gomathy ◽  
B. Susheela
Keyword(s):  
Benzoic Acid ◽  
Ferrous Sulfate ◽  
Xylenol Orange ◽  
Radiation Chemistry

The radiation chemistry of aqueous ferrous sulfate solutions at natural pH

1983 ◽  
Vol 36 (7) ◽  
pp. 1305 ◽  
Author(s):  
RW Matthews
Keyword(s):  
Hydrogen Atom ◽  
Ferrous Sulfate ◽  
Experimental Error ◽  
Absorbed Dose ◽  
Radiation Chemistry ◽  
Ion Concentration ◽  
Sulfate Solutions ◽  
Diffusion Controlled ◽  
Wide Range ◽  
Γ Rays

The yield of FeIII species has been determined in FeSO4 solutions irradiated at natural pH with 60Co γ-rays for a wide range of solute conditions. The stoichiometry of the hydrogen peroxide reaction was investigated and found to be abnormal if H2O2 is present in excess. If, however, FeS04 is present in excess, as it is in the irradiation of FeSO4 solutions, deviations from the normal stoichiometry are trivial. In nitrous oxide saturated solutions initial G(FeIII) values were found to be from 6.90 to 7.72 for FeSO4 concentrations in the range (0.5-2.0) × 10-3 M. Non-linearity in the yield of ferric ion concentration against dose plots was attributed to competition between hydrogen atom reduction of ferric species with hydrogen atom oxidation of ferrous species. The reaction between hydrogen atom and the ferric species was estimated to be close to diffusion controlled. In aerated solutions, the FeIII yield was, within experimental error, a linear function of dose for FeSO4 concentrations in the range (0.5 - 2.0) × 10.-3 M with G(FeIII) values of 12.27 ± 0.06, 12.62 ± 0.07 and 12.77 ± 0.10 for 0.5, 1.0 and 2.0 × M respectively. At lower FeSO4 concentrations. deviation from linearity was noticeable. The deviation was attributed to competition between FeII and FeIII species for the O2- radical anion. k(O2-· + FeII)/k(O2-·+ FeIII) was determined to be about 4.0. In deaerated solu- tion, the FeIII yield against absorbed dose for 1 × M FeSO4 solution was followed to extended doses. A limiting FeIII yield of about 0.75 times the aerated solution yield was observed in the closed system. The data were quite well described by values calculated from the reaction mechanism, published rate constants and the rate ratio of 0.016 for k(H· + FeII)/k(H· + FeIII) determined from the N2O experiments, and demonstrate the importance of reducing radical reactions with insoluble ferric species.

The Radiation Chemistry of Aqueous Ferrous Sulfate-Benzoic Acid Solutions

1963 ◽  
Vol 20 (2) ◽  
pp. 263 ◽  
Author(s):  
Janet Geisselsoder ◽  
Mary Jane Kingkade ◽  
John S. Laughlin
Keyword(s):  
Benzoic Acid ◽  
Ferrous Sulfate ◽  
Radiation Chemistry ◽  
Acid Solutions

Radiation Chemistry

1975 ◽  
Vol 94 (4-6) ◽  
pp. 333-333
Author(s):  
K.-D. Asmus
Keyword(s):  
Radiation Chemistry
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