4.6 Article

Kinetics and Mechanism for the Sonochemical Degradation of a Nonionic Surfactant

Journal

JOURNAL OF PHYSICAL CHEMISTRY A
Volume 113, Issue 12, Pages 2865-2872

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp808968e

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Funding

  1. David Hay Memorial Fund
  2. Particulate Fluids Processing Centre
  3. Australian Research Council

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The sonolytic degradation of the nonionic surfactant, octaethylene glycol monododecyl ether (C12E8), has been studied at various initial concentrations below and above its critical micelle concentration (CMC). It has been observed that the degradation rate increases with an increase in the initial concentration of the surfactant until the CMC is reached. Above the CMC an almost constant degradation rate is observed, suggesting that the surfactant in its monomer form is involved in the degradation process. The degradation process of C12E8 involves two distinct primary processes occurring at the bubble/solution interface: (a) hydroxylation/oxidation of the surfactant and (b) pyrolytic fragmentation of the surfactant. The oxidative cleavage of ethylene oxide units provides evidence for OH radical attack. Hydroxylation of the ethoxy chain gives rise to various short-chain carboxyalkyl-polyethylene glycol intermediates. The polyethylene glycol chain formed, due to the scission of the C12E8 molecule, undergoes rapid hydroxylation/oxidation to yield simple compounds that have the potential to undergo further degradation. The detection of multiple intermediates indicates that several processes affect the complete degradation pathways of the surfactant molecule. TOC analysis, however, indicates that the sonolytic mineralization of the surfactant is difficult to achieve at reasonable rates due to the relatively low surface activity of the degradation products formed during sonolysis.

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