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Ashokkumar, M.; Grieser, F.; Vinodgopal, K.
Radiation 2000 incorporating the 20th AINSE Radiation Chemistry Conference and the 17th Radiation Biology Conference. Conference Handbook2000
Radiation 2000 incorporating the 20th AINSE Radiation Chemistry Conference and the 17th Radiation Biology Conference. Conference Handbook2000
AbstractAbstract
[en] Full text: The ultrasound induced decomposition of a commercially available polydisperse nonylphenol ethoxylate surfactant (Teric GN9) has been investigated. Nearly 90% mineralization and/or degradation into volatile products of the surfactant is achieved after sonication for 24 hours. Ultrasound has been found to be a useful tool to achieve a number of chemical processes. Linear and branched alkyl benzene sulfonates and alkyl nonylphenol ethoxylates are widely used surfactants which accumulated in the environment and contribute to a well-recognised pollution problem. We have investigated the use of ultrasound in the degradation of both types of surfactants with the aim of understanding the mechanism of degradation in order to optimise the decomposition process. In this presentation, we report on the sonochemical degradation of Teric GN9- polydisperse, a nonylphenol ethoxylate with an average of 9 ethylene oxide units. The ultrasound unit used for the degradation studies of the surfactant solutions was an Allied Signal (ELAC Nautik) RF generator and transducer with a plate diameter of 54.5 mm operated at 363 kHz in continuous wave mode at an intensity of 2 W/cm2. Ultrasound induced cavitation events generate primary radicals inside gas/vapour filled bubbles. Due to the extreme conditions (T ∼ 5000 K; P ∼ 100 atm) generated within the collapsing bubble, H and OH radicals are produced by the homolysis of water molecules, if water is the medium of sonication. These primary radicals attack the surfactant molecules adsorbed at the bubble/water interface. The initial rate of reaction of the surfactant was found to be dependent on the monomer concentration in solution below and above the critical micelle concentration of the surfactants. This result strongly suggests that the initial radical attack on the surfactants occurs at the cavitation bubble/solution interface, followed by oxidative decomposition and pyrolysis of volatile fragments of the surfactant within the bubble. Complete mineralisation/decomposition has been found to be a slow process. Evidence will be provided during the presentation to support these arguments
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Australian Institute of Nuclear Science and Engineering, Lucas Heights, NSW (Australia); 60 p; ISBN 0 9577217 3 0;
; 2000; p. 4; Radiation 2000; Lucas Heights, NSW (Australia); 26-28 Nov 2000; Available in abstract form only, full text entered in this record

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