High-energy ionising radiation initiated decomposition of acetovanillone

Research output: Article

9 Citations (Scopus)


Hydroxyl radical, hydrated electron and hydrogen atom intermediates of water radiolysis react with acetovanillone with rate coefficients of (1.05±0.1)×10 10, (3.5±0.5)×10 9 and (1.7±0.2)×10 10mol -1dm 3s -1. Hydroxyl radical and hydrogen atom attach to the ring forming cyclohexadienyl type radicals. The hydroxyl-cyclohexadienyl radical formed in hydroxyl radical reaction in dissolved oxygen free solution partly transforms to phenoxyl radical. In the presence of O 2 phenoxyl radical formation and ring destruction are observed. Hydrated electron in O 2 free solution attaches to the carbonyl oxygen and undergoes protonation yielding benzyl type radical. In air saturated 0.5mmoldm -3 solution using 15kGy dose most part of acetovanillone is degraded, for complete mineralisation five times higher dose is required. The experiments clearly show that acetovanillone can be efficiently removed from water by applying irradiation technology.

Original languageEnglish
Pages (from-to)1495-1498
Number of pages4
JournalRadiation Physics and Chemistry
Issue number9
Publication statusPublished - szept. 1 2012

ASJC Scopus subject areas

  • Radiation

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