4.8 Article

Hydroxyl radical dominated degradation of aquatic sulfamethoxazole by Fe0/bisulfite/O2: Kinetics, mechanisms, and pathways

Journal

WATER RESEARCH
Volume 138, Issue -, Pages 323-332

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2017.12.046

Keywords

Sulfamethoxazole (SMX); Fe-0; Bisulfite (S(IV)); Chemical calculation; Degradation pathways

Funding

  1. National Natural Science Foundation of China [51678188]
  2. State Key Laboratory of Urban Water Resource and Environment [2017DX04]

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In this study, batch experiments were carried out to investigate the key factors on sulfamethoxazole (SMX) removal kinetics in a new AOPs based on the combination of zero valent iron (Fe-0) and bisulfite (S(IV)). With the increase of Fe-0 from 0.25 mM to 5 mM, the removal rate of SMX was linearly increased in the Fe-0/S(IV)/O-2 system by accelerating the activation of S(IV) and Fe-0 corrosion to accelerate. In the first 10 min of reaction, the increasing concentration of S(IV) inhibited SMX removal after since the high S(IV) concentration quenched reactive oxidative species (ROS). Then SMX removal rate was accelerated with the increase of S(IV) concentration after S(IV) were consumed up The optimal ratio of S(IV) concentrations to Fe-0 concentration for SMX removal in the Fe-0/S(IV)/O-2 system was 1:1. With SMX concentrations increasing from 1 to 50 mu M, SMX removal rate was inhibited for the limitation of ROS yields. Although the presence of center dot SO4- and center dot OH was confirmed by electron paramagnetic resonance (EPR) spectrum, center dot OH was identified as the dominant ROS in the Fe-0/S(IV)/O-2 system by chemical quenching experiments. Besides, strong inhibitive effects of 1,10-phenanthroline on SMX degradation kinetics by Fe-0/S(IV)/O-2 proved that the generation of ROS was rely on the release of Fe(II) and Fe(III) The generation of center dot SO4- was ascribed to the activation of S(IV) by Fe(II)/Fe(III) recycling and the activation of HSO5- by Fe(II) And center dot OH was simultaneously transformed from center dot SO4- and generated by Fe-0/O-2. Density functional theory (DFT) calculation was conducted to reveal special reactive sites on SMX for radicals attacking and predicted intermediates. Finally, four possible SMX degradation pathways were accordingly proposed in the Fe-0/S(IV)/O-2 system based on experimental methods and DFT calculation. (C) 2018 Elsevier Ltd. All rights reserved.

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