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Removing Estrogenic Steroids from Waters: The Role of Reducing Hydrated Electron Reactions

  • Kimberly A. Rickman and Stephen P. Mezyk EMAIL logo
Published/Copyright: November 30, 2016
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Abstract

The presence of both synthetic and natural steroids in waters is currently one of the most pressing concerns to water treatment utilities. The use of radical-based advanced oxidation/reduction processes (AO/RPs) to augment standard water treatment methods may be of interest. In support of the application of these AO/RP rate constants have been determined for the reaction of the reducing hydrated electron (eaq-) with three important estrogenic steroids; ethinylestradiol, estradiol and progesterone. Absolute values of (1.46 ± 0.16) x 108, (2.52 ± 0.11) x 108 and (8.65 ± 0.15) x 109 M-1 s-1 were directly measured for these three steroids, respectively, using electron pulse radiolysis and absorption spectroscopy. Our value for estradiol is over a factor of 100 slower than the single previously reported rate constant for this compound determined using Co(en)33+ competition kinetics, suggesting that only minimal reduction for this steroid or ethinylestradiol occurs. The faster rate constant for progesterone indicates that the reduction predominantly occurs at its ketone moiety. These rate constants, which are the first direct hydrated electron rate constant measurements reported for estogenic steroids in water, indicate that in comparison to the much faster oxidizing radical reactions reduction will not be a significant destructive pathway in real-world contaminant water treatment.

Received: 2010-10-11
Revised: 2010-11-29
Accepted: 2010-12-1
Published Online: 2016-11-30
Published in Print: 2011-1-1

© 2016 by Walter de Gruyter Berlin/Boston

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