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ENR was aerobically removed within 5 min by goethite with adsorbed Fe(II), without especial irradiation and strong oxidants. The results of spin trap electron spin resonance (ESR) experiments provide evidence that Fe(II)/Fe(III) complexes facilitate the generation of •OH. The electrophilic attack by •OH opens the quinolone ring of ENR and initiates further transformation reactions. Five transformation products were identified using high performance liquid chromatography-quadrupole time-of-flight mass spectrometry and the ENR degradation process was proposed accordingly. The identification of ENR transformation products also revealed that both the surface adsorption and the electron density distribution in the molecule determined the reactive site and transformation pathway. This study highlights an important, but often underappreciated, natural process for in situ degradation of antibiotics. With the easy migration of the goethite-MR-1 complex to the anaerobic/aerobic interface, the environmental fates of ENR and other antibiotics need to be seriously reconsidered.
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Yan et al. (2016) studied this question.
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