Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

THE GAMMA RADIOLYSIS OF AQUEOUS AND ALCOHOLIC SOLUTIONS OF ORANGE IV. Thesis

Thesis/Dissertation ·
OSTI ID:4103722
The decolorization of deaerated aqueous solutions of Orange IV is the result of H atom and hydroxyl radical attacks. The H atoms are believed to add to the azo or amine N atoms and the hydroxyl radicals probably add to the aromatic C atoms. The decolorization when O is present initially is attributed to hydroxyl and hydroperoxyl radical additions until the O is consumed. The yields of the decolorization reactions in water are very low compared to the yields of H atoms and hydroxyl radicals formed. It was estimated that 10 to 14 radicals are required for each dye molecule decolorized. The dye molecule may serve as a site for the recombination of a H atom and a hydroxyl radical. Some funther oxidation appears after irradiation and is attributed to the hydrogen peroxide formed with a yield of G = 0.67. The decolorization of deaerated methanolic solutions of Orange IV results from its reduction to the hydrazo derivatives by the addition of H atoms, methylol, methyl, and hydroxyl radicals. The decolorization reaction in methanol containing O is inhibited until the O is consumed. Both reactions are discussed. The monoazo dye Orange I behaves in a similar manner to Orange IV when deaerated methanolic solutions are irradiated. The radical additions to the azo linkage apparently yield the derivatives of sodium sulfanilate and 4-amino-1-maphthol. The results obtained in ethanolic solutions are apparently analogous to those in methanolic solutions. The efficiency of the decolorization process is again high and indicates essentially 100% addition of the radicals to the azo linkage. The use of ionizing radiation in an organic synthesis is illustrated by this work. The principal limitation to this method is the mixture of products obtained from the random addition of the free radicals formed from the solvent. The process is easily performed and proceeds with a very high efficiency. (M.P.G.)
Research Organization:
Originating Research Org. not identified
NSA Number:
NSA-18-012249
OSTI ID:
4103722
Country of Publication:
Country unknown/Code not available
Language:
English