The Radiolysis of Aqueous Solutions at High Intensities

the presence of acid), hydrogen atoms, and hydroxyl radicals. These species are produced in localized regions along the track of the incident radiation. These regions of high radical concentrations expand, and while this process is occurring radical-radical reactions take place leading to hydrogen, hydrogen peroxide, and regenerated water, while radical-solute reactions will also occur to an extent depending on the reactivity and concentration of the solute and the state of expansion of the localized regions. Calculations by various workers (3-6) using the free radical theory have been quite successful in explaining many of the aspects of the radiation chemistry of aqueous systems. A point of uncertainty in the calculations has been the necessity to assume rate constants for the free radical reactions and to assume values for the parameters used to describe the heterogeneous distribution of the radicals produced, and their eventual diffusion and reaction. In the present work conditions were used such that intertrack reactions were important and the diffusion of the radicals from their tracks before chemical reaction took place was sufficient so that they may be considered as being produced homogeneously. An important factor in the irradiation procedure was that the radiation was produced in pulses of a duration such that no significant chemical reaction took place during the pulse. Thus at the end of such a pulse a known concentration of radicals was produced the subsequent reactions of which were described mathematically by normal homogeneous kinetics.

[1]  K. Scharf,et al.  Investigation of the spectrophotometric method of measuring the ferric ion yield in the ferrous sulfate dosimeter. , 1962, Radiation research.

[2]  E. Hart,et al.  RADIATION CHEMISTRY OF WATER WITH PULSED HIGH INTENSITY ELECTRON BEAMS1 , 1962 .

[3]  A. R. Anderson A CALORIMETRIC DETERMINATION OF THE OXIDATION YIELD OF THE FRICKE DOSIMETER AT HIGH DOSE RATES OF ELECTRONS1a , 1962 .

[4]  A. O. Allen,et al.  The radiation chemistry of water and aqueous solutions , 1961 .

[5]  H. C. Sutton,et al.  The effects of high dose rates of ionizing radiations on solutions of iron and cerium salts , 1960, Proceedings of the Royal Society of London. Series A. Mathematical and Physical Sciences.

[6]  J. M. Kennedy,et al.  THE KINETICS OF RADICAL REACTIONS IN THE TRACKS OF FAST ELECTRONS. A DETAILED STUDY OF THE SAMUEL-MAGEE MODEL FOR THE RADIATION CHEMISTRY OF WATER , 1958 .

[7]  J. P. Keene The oxidation of ferrous ammonium sulfate solutions by electron irradiation at high dose rates. , 1957, Radiation Research.

[8]  R. H. Schuler,et al.  Yield of the Ferrous Sulfate Radiation Dosimeter: An Improved Cathode‐Ray Determination , 1956 .

[9]  E. Hart Radiation chemistry of aqueous ferrous sulfate-cupric sulfate solutions; effect of gamma-rays. , 1955, Radiation research.

[10]  A. H. Samuel,et al.  Theory of Radiation Chemistry. II. Track Effects in Radiolysis of Water , 1953 .

[11]  C. Hochanadel EFFECTS OF COBALT $gamma$-RADIATION OF WATER AND AQUEOUS SOLUTIONS , 1952 .

[12]  E. Hart Mechanism of the γ-Ray Induced Oxidation of Formic Acid in Aqueous Solution , 1951 .

[13]  JOSEPH WEISS,et al.  Radiochemistry of Aqueous Solutions , 1944, Nature.